GMP Training Courses - Regulatory Affairs

ICH Q12 - Product Life Cycle Management

Berlin, Germany

13-14 November 2018

ICH Q12 - Product Life Cycle Management

Drug Master File Procedures in the EU, the US and Japan

Berlin, Germany

22-23 November 2018

Drug Master File Procedures in the EU, the US and Japan

How to provide Process Validation Data in a Regulatory Submission

Barcelona, Spain

27-28 November 2018

How to provide Process Validation Data in a Regulatory Submission

Setting Specifications and Acceptance Criteria

Barcelona, Spain

28-29 November 2018

Setting Specifications and Acceptance Criteria

Pharmaceutical Contracts: GMP and Legal Compliance

Berlin, Germany

13-14 February 2019

Pharmaceutical Contracts: GMP and Legal Compliance

Global Registration and Life Cycle Management of APIs

Berlin, Germany

12-14 March 2019

Global Registration and Life Cycle Management of APIs

How to write the Quality Part of an IMPD

Prague, Czech Republic

19-20 March 2019

How to write the Quality Part of an IMPD

Handling Changes and Variations

Copenhagen, Denmark

26-27 March 2019

Handling Changes and Variations

GMP meets Regulatory Affairs

Barcelona, Spain

21-22 May 2019

GMP meets Regulatory Affairs

API Regulatory Starting Materials

Barcelona, Spain

23-24 May 2019

API Regulatory Starting Materials

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